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iTRAQ 分析联合 EpCAM 和 αB-晶状体蛋白对乳腺癌淋巴转移的预后价值。

Prognostic value of biomarkers EpCAM and αB-crystallin associated with lymphatic metastasis in breast cancer by iTRAQ analysis.

机构信息

Department of Pathology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, China.

Key Laboratory of Translational Cancer Stem Cell Research, Hunan Normal University, Changsha, Hunan, China.

出版信息

BMC Cancer. 2019 Aug 23;19(1):831. doi: 10.1186/s12885-019-6016-3.

Abstract

BACKGROUND

Metastasis is responsible for the majority of deaths in a variety of cancer types, including breast cancer. Although several factors or biomarkers have been identified to predict the outcome of patients with breast cancer, few studies have been conducted to identify metastasis-associated biomarkers.

METHODS

Quantitative iTRAQ proteomics analysis was used to detect differentially expressed proteins between lymph node metastases and their paired primary tumor tissues from 23 patients with metastatic breast cancer. Immunohistochemistry was performed to validate the expression of two upregulated (EpCAM, FADD) and two downregulated (NDRG1, αB-crystallin) proteins in 190 paraffin-embedded tissue samples. These four proteins were further analyzed for their correlation with clinicopathological features in 190 breast cancer patients.

RESULTS

We identified 637 differentially regulated proteins (397 upregulated and 240 downregulated) in lymph node metastases compared with their paired primary tumor tissues. Data are available via ProteomeXchange with identifier PXD013931. Furthermore, bioinformatics analysis using GEO profiling confirmed the difference in the expression of EpCAM between metastases and primary tumors tissues. Two upregulated (EpCAM, FADD) and two downregulated (NDRG1, αB-crystallin) proteins were associated with the progression of breast cancer. Obviously, EpCAM plays a role in the metastasis of breast cancer cells to the lymph node. We further identified αB-crystallin as an independent biomarker to predict lymph node metastasis and the outcome of breast cancer patients.

CONCLUSION

We have identified that EpCAM plays a role in the metastasis of breast cancer cells to the lymph node. αB-crystallin, a stress-related protein that has recently been shown to be important for cell invasion and survival, was identified as a potential prognostic biomarker to predict the outcome of breast cancer patients.

摘要

背景

转移是包括乳腺癌在内的多种癌症类型患者死亡的主要原因。虽然已经确定了一些因素或生物标志物来预测乳腺癌患者的预后,但很少有研究用于确定与转移相关的生物标志物。

方法

使用定量 iTRAQ 蛋白质组学分析方法检测 23 例转移性乳腺癌患者的淋巴结转移与其配对原发性肿瘤组织之间差异表达的蛋白质。免疫组织化学用于验证在 190 例石蜡包埋组织样本中两种上调(EpCAM、FADD)和两种下调(NDRG1、αB-晶体蛋白)蛋白的表达。进一步分析这四种蛋白与 190 例乳腺癌患者临床病理特征的相关性。

结果

与配对的原发性肿瘤组织相比,我们在淋巴结转移中鉴定出 637 个差异调节蛋白(397 个上调和 240 个下调)。数据可通过 ProteomeXchange 获得,标识符为 PXD013931。此外,使用 GEO 分析证实了 EpCAM 在转移和原发性肿瘤组织之间表达的差异。两种上调蛋白(EpCAM、FADD)和两种下调蛋白(NDRG1、αB-晶体蛋白)与乳腺癌的进展有关。显然,EpCAM 在乳腺癌细胞向淋巴结转移中发挥作用。我们进一步确定 αB-晶体蛋白是预测乳腺癌患者淋巴结转移和预后的独立生物标志物。

结论

我们已经确定 EpCAM 在乳腺癌细胞向淋巴结转移中发挥作用。αB-晶体蛋白是一种应激相关蛋白,最近被证明对细胞侵袭和存活很重要,被鉴定为预测乳腺癌患者预后的潜在预后生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/def8/6708189/dff0cd2dc750/12885_2019_6016_Fig1_HTML.jpg

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